CA1047662A - Asbestos-free phenol-aldehyde molding composition - Google Patents
Asbestos-free phenol-aldehyde molding compositionInfo
- Publication number
- CA1047662A CA1047662A CA228,430A CA228430A CA1047662A CA 1047662 A CA1047662 A CA 1047662A CA 228430 A CA228430 A CA 228430A CA 1047662 A CA1047662 A CA 1047662A
- Authority
- CA
- Canada
- Prior art keywords
- composition
- weight
- asbestos
- phenol
- molding composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
An asbestos free, heat resistant phenolic molding composition comprising in admixture, a phenolic resin and a filler combination of aluminum silicate, talc and cellulose fibers.
An asbestos free, heat resistant phenolic molding composition comprising in admixture, a phenolic resin and a filler combination of aluminum silicate, talc and cellulose fibers.
Description
` -~ 8CH-1832 .
This invention relates to an asbestos free, heat resistant phenolic molding composition comprising in ad-mixture a phenolic resin and a filler combi~ation of aluminum silicate, talc and csllulose fibers.
Phenolic molding compositions have been available for many years and are generally made with an asbestos filler~
The asbestos is usad as a reinforcing fiber or as a reinforcing fillerO The asbestos providas the phenolic molding composition with increased mechanical, thermal and electrical properties.
However, the use of asbestos filled phenolics provides hazard to those exposed to this typa of material.
Tha standard for direct exposure to asbestos fibers is clearly detailed by the Department of Labor's Occupationàl Safety and Health Administration (OS~). Effects of exposure to personnel involved in the manufacture of phenolic molding compound in which raw asbestos is handled or pro~essed is well delineated. What is less obvious is the health hazard to personnel in shops that mold asbestos material and finish or machine the molded parts.
In order to comply with OSHA standards dealing with asbestos, th~ development of asbestos-frae phenolic Molding compositions which comply with the OS~A law is needed.
However, there are properties problems associated with eliminating asbestos from phenolic molding compositions. Two of the key properties effected are dimensional stability and heat resistance9 The heat resistance, mechanical and electrical properties of the non-asbestos phenolic molding compositions must be at least ~quivialent to ths asbestos-containing com-postions. Additionally, the moldability of khe non asbestos compositions must be equivalent ~o the asbestos-filLed compo-sitions. Since the same mold is used for asbestos and .... ~ - :
, ' '. :. '.
, 6~
non-asbestos compositions, the shrinkage of both types should be similar. In short, the non-asbestos compositions should not change normal operation procedures, at lea~t in a deleterio~s sense.
The non-asbestos filler combination of the instant invention satisfies this criteria.
This invention is directed to an asbestos-free heat re~istant phenolic molding composition comprising in admixturs, a phenolic resin and a filler combination of aluminum silicate, talc and cellulose fibers.
The fillex combination o~ the instant invantion when used with the phenolic resin provides a molding composition having heat re~istant properties bettar than an asbestos ~illed phenolic xesin composition. Also, heat deflection temperature and dielectric strength are greater using the filler combination of the instant invention in place of asbest~ in phenolic resins. Additionally, water absorption, arc resistance, tensile strength, flexural strength, flexural modulus, compr~ssive strength, Izod impact and drop ball impact properties of a phenolic resin with the filler combin-ation of the instant invention are comparable to an asbestos filled phenolic re~in compositionD
The phenolic resin employed in the practice of this invention is prefarably a phenol-aldehyde resin and ca~
be any phenol-aldehyde resin which is prepared by reacting from lass than ons mole to more than one mole of an aldehyde per mole of phenol under cextain conditions to provide a rssin. If lesæ than one mole of an aldehyde is us~d, the resin so produced is commonly cailed a novQlac. The novolac r9sin is g~nerally the type that can be inely grou,nd and requires blending thereof with an external cro~slinking agent such as h~xamethylenetetramine in order to provide a th~rmose table resin which can be advanced to an infusible
This invention relates to an asbestos free, heat resistant phenolic molding composition comprising in ad-mixture a phenolic resin and a filler combi~ation of aluminum silicate, talc and csllulose fibers.
Phenolic molding compositions have been available for many years and are generally made with an asbestos filler~
The asbestos is usad as a reinforcing fiber or as a reinforcing fillerO The asbestos providas the phenolic molding composition with increased mechanical, thermal and electrical properties.
However, the use of asbestos filled phenolics provides hazard to those exposed to this typa of material.
Tha standard for direct exposure to asbestos fibers is clearly detailed by the Department of Labor's Occupationàl Safety and Health Administration (OS~). Effects of exposure to personnel involved in the manufacture of phenolic molding compound in which raw asbestos is handled or pro~essed is well delineated. What is less obvious is the health hazard to personnel in shops that mold asbestos material and finish or machine the molded parts.
In order to comply with OSHA standards dealing with asbestos, th~ development of asbestos-frae phenolic Molding compositions which comply with the OS~A law is needed.
However, there are properties problems associated with eliminating asbestos from phenolic molding compositions. Two of the key properties effected are dimensional stability and heat resistance9 The heat resistance, mechanical and electrical properties of the non-asbestos phenolic molding compositions must be at least ~quivialent to ths asbestos-containing com-postions. Additionally, the moldability of khe non asbestos compositions must be equivalent ~o the asbestos-filLed compo-sitions. Since the same mold is used for asbestos and .... ~ - :
, ' '. :. '.
, 6~
non-asbestos compositions, the shrinkage of both types should be similar. In short, the non-asbestos compositions should not change normal operation procedures, at lea~t in a deleterio~s sense.
The non-asbestos filler combination of the instant invention satisfies this criteria.
This invention is directed to an asbestos-free heat re~istant phenolic molding composition comprising in admixturs, a phenolic resin and a filler combination of aluminum silicate, talc and cellulose fibers.
The fillex combination o~ the instant invantion when used with the phenolic resin provides a molding composition having heat re~istant properties bettar than an asbestos ~illed phenolic xesin composition. Also, heat deflection temperature and dielectric strength are greater using the filler combination of the instant invention in place of asbest~ in phenolic resins. Additionally, water absorption, arc resistance, tensile strength, flexural strength, flexural modulus, compr~ssive strength, Izod impact and drop ball impact properties of a phenolic resin with the filler combin-ation of the instant invention are comparable to an asbestos filled phenolic re~in compositionD
The phenolic resin employed in the practice of this invention is prefarably a phenol-aldehyde resin and ca~
be any phenol-aldehyde resin which is prepared by reacting from lass than ons mole to more than one mole of an aldehyde per mole of phenol under cextain conditions to provide a rssin. If lesæ than one mole of an aldehyde is us~d, the resin so produced is commonly cailed a novQlac. The novolac r9sin is g~nerally the type that can be inely grou,nd and requires blending thereof with an external cro~slinking agent such as h~xamethylenetetramine in order to provide a th~rmose table resin which can be advanced to an infusible
-2-~ 8CH-1832 6~i~
state upon exposure to elevated temperatures~ Whila any external crosslinking agent can be amploye~ herein, the preferred extexnal crosslinking agent is hexamethylenetetramine.
Generally, the preferred range of aldehyde employed herain to prepare the novolac is 0.5-0.9 moles thereo~ per mole of phenol and preferably 0~6-0.8 moles thereoE. While any aldehyde can be employad herein such as formaldahyde, paraformaldahydo, acetaldehyde, butyraldahyde, urfuraldchyde, etc., the preferred aldahy~e to be employed herein is formal- ;-dehyde.
.: . .
When employing more than one mole of aldehyde per mole of phenol, a one-staga resin is produced which ~an be advanced to an infusible state by the mere application of elevated temperatures. The one-stage resin which can be employed herein i9 one prepared by reacting more than one mole of an aldehyde per mole of phenol and preferably 1.1~3.0 moles thereof. Again, the preferred aldehyde is formaldehyde.
In addition, it has also been observed that when using a phenol-formaldehyde novolac, favorable molding characteristics are obtained when the novolac has ortho-ortho content of less than 70 weight percent of the total novolac composition. Optimum rssults are obtained when the ortho-ortho content is around 50 weight percent, the balance of the novolac consists of ortho-para and para-para linkages.
By these various types of linkage, it is meant the methylene bridging between the phenol nuclei and can be represented by the fol~owi~g formulas:
.: , . .
, , ' ': .
..... .
... ...
. ...
... ..
state upon exposure to elevated temperatures~ Whila any external crosslinking agent can be amploye~ herein, the preferred extexnal crosslinking agent is hexamethylenetetramine.
Generally, the preferred range of aldehyde employed herain to prepare the novolac is 0.5-0.9 moles thereo~ per mole of phenol and preferably 0~6-0.8 moles thereoE. While any aldehyde can be employad herein such as formaldahyde, paraformaldahydo, acetaldehyde, butyraldahyde, urfuraldchyde, etc., the preferred aldahy~e to be employed herein is formal- ;-dehyde.
.: . .
When employing more than one mole of aldehyde per mole of phenol, a one-staga resin is produced which ~an be advanced to an infusible state by the mere application of elevated temperatures. The one-stage resin which can be employed herein i9 one prepared by reacting more than one mole of an aldehyde per mole of phenol and preferably 1.1~3.0 moles thereof. Again, the preferred aldehyde is formaldehyde.
In addition, it has also been observed that when using a phenol-formaldehyde novolac, favorable molding characteristics are obtained when the novolac has ortho-ortho content of less than 70 weight percent of the total novolac composition. Optimum rssults are obtained when the ortho-ortho content is around 50 weight percent, the balance of the novolac consists of ortho-para and para-para linkages.
By these various types of linkage, it is meant the methylene bridging between the phenol nuclei and can be represented by the fol~owi~g formulas:
.: , . .
, , ' ': .
..... .
... ...
. ...
... ..
-3-: "' , .
.. ~,, '. .
~~~ 8CH-1832 ~
~ 766;i~
_ i A~ OH OH
~ ~_C~2~
ortho-ortho linkage ;: .
B~ OH
~ _ CH2 _ . ...
ortho-para~1inkage IH
T ~
l ..
o~ ... .
~: ~ para-para linkage :~ The individual compone~ts of the combination of ::
fillers of the instant invention, i~e., alumina silicake, -~
talc and cellulose fibers are commercially availab:Le in~ :
~ariou~ forms and grades. The combination o~ fillers can ~:
be employed in an amount of from ab~ut 15 to about 50 weight '~
; -4-~ 47~?~ %
parcent~ Preferably the filler combination contains from ab~ut S to about 20 weight percent alumina silicate, from about 5 to about 20 weight percent of talc and from about 5 to about 10 weight percent of cellulose fibers~ Said weight percents being based on the weight of the molding composition.
The composition of this invention is prepared by msthods well known to those skilled in the art~ For example, -.
the indi~idual ingredisnts are mixed together in a suitable vessel and then fed directly to the feed hopper of a screw extruder or roll mill~ :
It should be noted that the phenolic resin ~ .
compositions of this invention can, and generally do, have present additive compounds which are normally used in such compositions in addition to the composition of this invention.
Included among these other additives are fillers such as wood flour, clacium carbonate, glass fibers, etc. and any combination of thess or other known ~illers employed in the phenolic molding composition as well as such additives as coal~ lime, stearic acid, etc. I~ a preferred embodiment of the instant invention, the composition of the instant invention may contain lime in amounts of from 4 to 10 weight percent. In yet another preferred embodiment the composition of the instant inv~ntion may contain coal in amounts of from .~ .
5 to 15 weight percent~
. .
The following examples are set orth to illustrate more clearly the prin~iple and practice of this invention to ~ ...
those skillad in the art and unless otherwi~e ~pecifi~d, wh~re parts vr percentages are mentioned,.they are parts or ...
percentages by weightO ~ :
A phenol-formaldehyde re~in is preparad by reacting ;.
about 0.7 moles o~ ~ormaldehyde per mole o~ phenol in the -5- ;
' presence of an acid catalyst, whieh is subsequently neutralized, tor form a novolac.
The novolac is ground to a fine p,article size with about 16 weight percent of hexamethylenetetramine based on the weight of novolac.
The resin mixture is then blendad with 38 weight perc~nt of asbastos fibers and 15 weight percent of wood flour to form a 50/50 mixture. Tha bland is then compounded in a screw extruder at a~out 220F which is sufficient to melt the resin. The molten mixture is advanced through the screw and extruded into granular or pellet form.
EXAMPLE II
Example I is repeatad except that a filler com-bination of 14 weight percent aluminum silicate, 15 weight percent o~ talc and 8 weight percent of cellulos~ fiber i9 used in place of tha asbe~tosO
Each of tho materials so prapared in Examples I ~:-and II are subjected to the following tests: Water Absorption, Hsat Deflection (ASTM D-648), Dielectric Strength (AST~ D-149), Arc Resistance (ASTM D-495), Tensile Strsngth (ASTM D-6Sl), Flexural Strength (ASTM D-~i90)o Flexural ~odulus (ASTM D-790), :: . .
Compressive Strength (ASTM D-695), Izod Impact (ASTM D-256A) .;-and the Drop Ball Impact. All test sp~cimens are m~lded from :
conventional molding methods~ Thc results are tabulated as follows:
T~BLE I ~
T0st Example I ~ Dæ~_E~ :~
Wat~r Absorption~%, 24 hr.) 0.2 0.2 ~ :
H~at Deflectio~( F,~ 264 psi) 380 350 Dielectric Strength(60 cps,25C,st. VPM) 360 350 Arc Re~ista~t (Bect 180 180 Ten~ils Strength (psi) 7000 8000 Flexural Streng~h (psi~ 12000 12000 6 Fle~ural Modulu~ ~psi) 1 x 10~ 1 x 10 Compressive Strength (psi) 23000 27000 I7~od Impact(ft-lb/i~.notch) ~30 O33 :
Drop Ball Impact (in4 1/4 lb. weight) 11 13 . . .
8CH-1832 :
~ IL76~
Dimensional stability refers to tha ability of the molded part to maintain its dimensions within reasonable limits under a wide variety of ambient conditions; it is particularly important when the molded phenolic part is a component in a device or assembly which must raly on close part tolerances for successful operation.
This property was evaluated for the compositions of Examples I and II. The test moldings, in this casa, were compression molded 1 1/2 in. x 3 in. rectangular boxes, 3/4 in~ deep, with cross sections of OolOO in. (walls) and 1/8 in. and 1/4 in. (bottom).
Dimensions in both the length and width dire~tion were tracked ov~r a period of 15 days at room temperature, 150F, 200F and 250F.
The results are tabulated as follows:
TABLE II
Tem~erature Example I* ~3Eæ~æ_LE~
Room Temperature (75F) 0~1 0.2 :
150F 1~4 1.3 200F 2.3 2.6 : : .
250F 2~9 3.4 *Th~e numb~rs indicat0 dimensional change of length in mil~ per inch.
The results in Table I demonstrate that heat de-flection and dielectric strength were significantly improved with the composition of Example I whereas water absorptionr arc resistance, tensila strength, flexural strength, flexural modulus, compressive strength, Izod impact and drop ball . :~
impact data o~ Example I were comparable wi~h Exampls II.
Table II demonstrates that at higher temperatures the composition :
of Example 1 sxhibits less overall change in dimension than -~
the composition of Example II~ Therefore, the filler : ~:
combination of the instant invention provides a ph~nolic mold- ::
ing composition of comparable and better properties than ;
a composition containing a~bestos.
,: i , ~ : : - . . .. ..
Example II was repeated using varying amounts of the aluminum silicate, talc and cellulose fibers. The results obtained were similar to those sat forth in Tables I and II.
Obviously, other modifications and variations of the p.resent invention are possible in the light of the abovs teachings. It is, therafore, to be understood that changes may be made in the particular embodiments described which are within the full intended scopa o~ ths :invention as defined by the appended claims.
.. ~,, '. .
~~~ 8CH-1832 ~
~ 766;i~
_ i A~ OH OH
~ ~_C~2~
ortho-ortho linkage ;: .
B~ OH
~ _ CH2 _ . ...
ortho-para~1inkage IH
T ~
l ..
o~ ... .
~: ~ para-para linkage :~ The individual compone~ts of the combination of ::
fillers of the instant invention, i~e., alumina silicake, -~
talc and cellulose fibers are commercially availab:Le in~ :
~ariou~ forms and grades. The combination o~ fillers can ~:
be employed in an amount of from ab~ut 15 to about 50 weight '~
; -4-~ 47~?~ %
parcent~ Preferably the filler combination contains from ab~ut S to about 20 weight percent alumina silicate, from about 5 to about 20 weight percent of talc and from about 5 to about 10 weight percent of cellulose fibers~ Said weight percents being based on the weight of the molding composition.
The composition of this invention is prepared by msthods well known to those skilled in the art~ For example, -.
the indi~idual ingredisnts are mixed together in a suitable vessel and then fed directly to the feed hopper of a screw extruder or roll mill~ :
It should be noted that the phenolic resin ~ .
compositions of this invention can, and generally do, have present additive compounds which are normally used in such compositions in addition to the composition of this invention.
Included among these other additives are fillers such as wood flour, clacium carbonate, glass fibers, etc. and any combination of thess or other known ~illers employed in the phenolic molding composition as well as such additives as coal~ lime, stearic acid, etc. I~ a preferred embodiment of the instant invention, the composition of the instant invention may contain lime in amounts of from 4 to 10 weight percent. In yet another preferred embodiment the composition of the instant inv~ntion may contain coal in amounts of from .~ .
5 to 15 weight percent~
. .
The following examples are set orth to illustrate more clearly the prin~iple and practice of this invention to ~ ...
those skillad in the art and unless otherwi~e ~pecifi~d, wh~re parts vr percentages are mentioned,.they are parts or ...
percentages by weightO ~ :
A phenol-formaldehyde re~in is preparad by reacting ;.
about 0.7 moles o~ ~ormaldehyde per mole o~ phenol in the -5- ;
' presence of an acid catalyst, whieh is subsequently neutralized, tor form a novolac.
The novolac is ground to a fine p,article size with about 16 weight percent of hexamethylenetetramine based on the weight of novolac.
The resin mixture is then blendad with 38 weight perc~nt of asbastos fibers and 15 weight percent of wood flour to form a 50/50 mixture. Tha bland is then compounded in a screw extruder at a~out 220F which is sufficient to melt the resin. The molten mixture is advanced through the screw and extruded into granular or pellet form.
EXAMPLE II
Example I is repeatad except that a filler com-bination of 14 weight percent aluminum silicate, 15 weight percent o~ talc and 8 weight percent of cellulos~ fiber i9 used in place of tha asbe~tosO
Each of tho materials so prapared in Examples I ~:-and II are subjected to the following tests: Water Absorption, Hsat Deflection (ASTM D-648), Dielectric Strength (AST~ D-149), Arc Resistance (ASTM D-495), Tensile Strsngth (ASTM D-6Sl), Flexural Strength (ASTM D-~i90)o Flexural ~odulus (ASTM D-790), :: . .
Compressive Strength (ASTM D-695), Izod Impact (ASTM D-256A) .;-and the Drop Ball Impact. All test sp~cimens are m~lded from :
conventional molding methods~ Thc results are tabulated as follows:
T~BLE I ~
T0st Example I ~ Dæ~_E~ :~
Wat~r Absorption~%, 24 hr.) 0.2 0.2 ~ :
H~at Deflectio~( F,~ 264 psi) 380 350 Dielectric Strength(60 cps,25C,st. VPM) 360 350 Arc Re~ista~t (Bect 180 180 Ten~ils Strength (psi) 7000 8000 Flexural Streng~h (psi~ 12000 12000 6 Fle~ural Modulu~ ~psi) 1 x 10~ 1 x 10 Compressive Strength (psi) 23000 27000 I7~od Impact(ft-lb/i~.notch) ~30 O33 :
Drop Ball Impact (in4 1/4 lb. weight) 11 13 . . .
8CH-1832 :
~ IL76~
Dimensional stability refers to tha ability of the molded part to maintain its dimensions within reasonable limits under a wide variety of ambient conditions; it is particularly important when the molded phenolic part is a component in a device or assembly which must raly on close part tolerances for successful operation.
This property was evaluated for the compositions of Examples I and II. The test moldings, in this casa, were compression molded 1 1/2 in. x 3 in. rectangular boxes, 3/4 in~ deep, with cross sections of OolOO in. (walls) and 1/8 in. and 1/4 in. (bottom).
Dimensions in both the length and width dire~tion were tracked ov~r a period of 15 days at room temperature, 150F, 200F and 250F.
The results are tabulated as follows:
TABLE II
Tem~erature Example I* ~3Eæ~æ_LE~
Room Temperature (75F) 0~1 0.2 :
150F 1~4 1.3 200F 2.3 2.6 : : .
250F 2~9 3.4 *Th~e numb~rs indicat0 dimensional change of length in mil~ per inch.
The results in Table I demonstrate that heat de-flection and dielectric strength were significantly improved with the composition of Example I whereas water absorptionr arc resistance, tensila strength, flexural strength, flexural modulus, compressive strength, Izod impact and drop ball . :~
impact data o~ Example I were comparable wi~h Exampls II.
Table II demonstrates that at higher temperatures the composition :
of Example 1 sxhibits less overall change in dimension than -~
the composition of Example II~ Therefore, the filler : ~:
combination of the instant invention provides a ph~nolic mold- ::
ing composition of comparable and better properties than ;
a composition containing a~bestos.
,: i , ~ : : - . . .. ..
Example II was repeated using varying amounts of the aluminum silicate, talc and cellulose fibers. The results obtained were similar to those sat forth in Tables I and II.
Obviously, other modifications and variations of the p.resent invention are possible in the light of the abovs teachings. It is, therafore, to be understood that changes may be made in the particular embodiments described which are within the full intended scopa o~ ths :invention as defined by the appended claims.
Claims (6)
1. An asbestos free, heat resistant thermosettable phenol-aldehyde molding composition comprising in admixture, a 85-50 weight percent phenol-aldehyde resin and correspondingly 15-50 weight percent of a filler combination of aluminum silicate, talc and cellulose fibers, said aluminum silicate being present in about 5-20 parts by weight, said talc being present in about 5-20 parts by weight, said cellulose fibers being present in about 5-10 parts by weight, said parts being based on the weight of said molding composition.
2. The composition as defined in claim 1 wherein the filler combination is present in an amount of about 37 weight percent based on the weight of the molding composition.
3. The composition as defined in claim 1 or 2 wherein the aluminum silicate, said talc and said cellulose fibers are present in a proportion of about 14:15:8.
4. The composition as defined in claim 1 or 2 wherein saidphenol-aldehyde resin is a phenol-formaldehyde novolac containing about 16 percent by weight curing agent based on the weight of said novolac.
5. The composition as defined in claim 1 which contains lime.
6. The composition as defined in claim 1 which contains coal.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US478785A US3922241A (en) | 1974-06-12 | 1974-06-12 | Asbestos-free heat-resistant thermosettable phenol-aldehyde molding composition |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1047662A true CA1047662A (en) | 1979-01-30 |
Family
ID=23901342
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA228,430A Expired CA1047662A (en) | 1974-06-12 | 1975-06-02 | Asbestos-free phenol-aldehyde molding composition |
Country Status (9)
Country | Link |
---|---|
US (1) | US3922241A (en) |
JP (1) | JPS5761053B2 (en) |
AR (1) | AR204583A1 (en) |
BR (1) | BR7503715A (en) |
CA (1) | CA1047662A (en) |
DE (1) | DE2525796C2 (en) |
FR (1) | FR2274653A1 (en) |
GB (1) | GB1510991A (en) |
IT (1) | IT1038833B (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5320529U (en) * | 1976-07-30 | 1978-02-21 | ||
US4130537A (en) * | 1977-02-02 | 1978-12-19 | H. K. Porter Company, Inc. | Asbestos free friction element |
US4119591A (en) * | 1977-07-05 | 1978-10-10 | The Bendix Corporation | Friction material reinforced with steel and cellulose fibers |
FR2396832A1 (en) * | 1977-07-08 | 1979-02-02 | Redco Sa | COMPOSITION OF MATERIAL BASED ON MINERAL FIBERS |
US4217255A (en) * | 1977-07-14 | 1980-08-12 | Abex Corporation | Composition railroad friction material with synthetic fiber content |
US4197223A (en) * | 1977-08-10 | 1980-04-08 | Ferodo Limited | Asbestos free friction materials |
US4242241A (en) * | 1977-10-31 | 1980-12-30 | The Celotex Corporation | Method for making a slurry containing particulate matter and fibers for a preformed insulation product |
US4233203A (en) * | 1977-12-22 | 1980-11-11 | Hooker Chemicals & Plastics Corp. | Moldable thermosetting phenol-aldehyde resin compositions and process for making the compositions |
US4373037A (en) * | 1981-05-29 | 1983-02-08 | Engelhard Corporation | Asbestos-free friction material incorporating attapulgite clay |
JPS59149947A (en) * | 1983-02-15 | 1984-08-28 | Matsushita Electric Works Ltd | Phenolic resin molding material |
US5464513A (en) * | 1994-01-11 | 1995-11-07 | Scientific Utilization, Inc. | Method and apparatus for water decontamination using electrical discharge |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1218568A (en) * | 1965-12-28 | 1971-01-06 | Foseco Trading Ag | Mould linings |
US3658750A (en) * | 1969-02-13 | 1972-04-25 | Hitachi Ltd | Thermosetting resin composition and electrical appliances using the same |
FR2193077B1 (en) * | 1972-07-18 | 1976-06-11 | Lievremont Henri |
-
1974
- 1974-06-12 US US478785A patent/US3922241A/en not_active Expired - Lifetime
-
1975
- 1975-01-01 AR AR258783A patent/AR204583A1/en active
- 1975-05-16 GB GB20863/75A patent/GB1510991A/en not_active Expired
- 1975-06-02 CA CA228,430A patent/CA1047662A/en not_active Expired
- 1975-06-09 FR FR7517863A patent/FR2274653A1/en active Granted
- 1975-06-10 IT IT24195/75A patent/IT1038833B/en active
- 1975-06-10 DE DE2525796A patent/DE2525796C2/en not_active Expired
- 1975-06-11 BR BR4770/75D patent/BR7503715A/en unknown
- 1975-06-11 JP JP50069757A patent/JPS5761053B2/ja not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB1510991A (en) | 1978-05-17 |
US3922241A (en) | 1975-11-25 |
FR2274653B1 (en) | 1979-03-23 |
JPS5761053B2 (en) | 1982-12-22 |
BR7503715A (en) | 1976-07-06 |
DE2525796C2 (en) | 1983-12-01 |
IT1038833B (en) | 1979-11-30 |
FR2274653A1 (en) | 1976-01-09 |
AR204583A1 (en) | 1976-02-12 |
DE2525796A1 (en) | 1976-01-02 |
JPS518359A (en) | 1976-01-23 |
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